about
Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology.GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.A Rare Variant Identified Within the GluN2B C-Terminus in a Patient with Autism Affects NMDA Receptor Surface Expression and Spine Density.Cryo-EM structures of the triheteromeric NMDA receptor and its allosteric modulation.GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function.Positive Modulatory Interactions of NMDA Receptor GluN1/2B Ligand Binding Domains Attenuate Antagonists Activity.Glutamate Genetics in Obsessive-Compulsive Disorder: A Review.Hypoxia-ischemia modifies postsynaptic GluN2B-containing NMDA receptor complexes in the neonatal mouse brain.The bioactive protein-ligand conformation of GluN2C-selective positive allosteric modulators bound to the NMDA receptor.Maternal Chronic Folate Supplementation Ameliorates Behavior Disorders Induced by Prenatal High-Fat Diet Through Methylation Alteration of BDNF and Grin2b in Offspring Hippocampus.De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.Functional Evaluation of a De Novo GRIN2A Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy.Rescue of learning and memory deficits in the human non-syndromic intellectual disability cereblon knockout mouse model by targeting the AMPK-mTORC1 translational pathway.Modulating GluN2B for the Treatment of Neurological and Psychiatric Disorders.The LILI Motif of M3-S2 Linkers Is a Component of the NMDA Receptor Channel Gate.Surface Expression, Function, and Pharmacology of Disease-Associated Mutations in the Membrane Domain of the Human GluN2B Subunit.Properties of Triheteromeric N-Methyl-d-Aspartate Receptors Containing Two Distinct GluN1 Isoforms.Disruption of GRIN2B Impairs Differentiation in Human NeuronsToward the Language OscillogenomeA genome-wide association study for harness racing success in the Norwegian-Swedish coldblooded trotter reveals genes for learning and energy metabolismAtypical Rett Syndrome and Intractable Epilepsy With Novel MutationGenomics in neurodevelopmental disorders: an avenue to personalized medicineA structurally derived model of subunit-dependent NMDA receptor function
P2860
Q36251183-0668A92E-C486-4BDB-8A02-DB8A0A0D3E07Q38854549-6BFB4083-60FB-49F5-8D91-8B4BEF43E134Q38914044-CF2AE4F1-D3B3-4349-BE5B-5AFB5F1E27E6Q41502069-8081DE57-F317-4250-AFB9-BE69772B67F8Q42140574-A9D60B99-4103-45D5-89B8-F049CA9FAB09Q42282637-C6D14CD7-561C-42B8-9950-E67CE48D26C1Q46461702-8DA909A1-F51E-4348-9E02-28F7339A6BF1Q46705286-FC2E23DE-E897-4781-A3E1-1D505AA38D9AQ47292153-B3F9209F-1F03-4AE9-8143-CBE312B2ABD5Q47635922-3AFCAEE0-1F47-48A3-BE05-CCCCC3ADA565Q47842300-8B6B52EF-45D0-4DE2-860D-621322B27CA8Q47879364-6B7BDF38-A2A5-4FB7-94E3-E5C10B9856A7Q48337984-2D08BA3C-B29A-42FC-9200-B419418F7D61Q49832999-F5093A96-7431-4F89-9031-FEADBFB101FAQ49838290-95CD5E1B-BCF4-4F57-861E-D7AACFEE437BQ52571507-15F7325B-6C16-4A56-9533-7265727BD81FQ52571510-17C8F2A4-A241-44BE-A6D2-9243439C016FQ52684491-77F830FC-DA3E-4980-968A-8E37589C84DBQ57040246-A80611BB-C910-45F7-B538-01C38E59B58AQ58574000-97E99824-0838-4DA3-A85A-C4E0CC83B7EEQ58696478-A6612227-E4BD-4702-AE5C-CAA74FB1979AQ58713846-BDA4B0B2-6B1B-4C19-87AF-9A7ACAEBFAB6Q58797492-3342C915-FD80-4586-AC0F-8182B4C459AFQ58805055-A7DC7EFA-9A5A-492D-A93A-D2D334EF0A9B
P2860
description
2016 nî lūn-bûn
@nan
2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Human GRIN2B variants in neurodevelopmental disorders
@ast
Human GRIN2B variants in neurodevelopmental disorders
@en
Human GRIN2B variants in neurodevelopmental disorders
@nl
type
label
Human GRIN2B variants in neurodevelopmental disorders
@ast
Human GRIN2B variants in neurodevelopmental disorders
@en
Human GRIN2B variants in neurodevelopmental disorders
@nl
prefLabel
Human GRIN2B variants in neurodevelopmental disorders
@ast
Human GRIN2B variants in neurodevelopmental disorders
@en
Human GRIN2B variants in neurodevelopmental disorders
@nl
P2093
P2860
P921
P3181
P1476
Human GRIN2B variants in neurodevelopmental disorders
@en
P2093
Hongjie Yuan
Scott J. Myers
Stephen F. Traynelis
Wenjuan Chen
P2860
P304
P3181
P356
10.1016/J.JPHS.2016.10.002
P407
P577
2016-10-01T00:00:00Z